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Illumina/Nextera Rapid Capture Exome (8 rxn x 12 plex)/FC-140-1003/1 Ea

  
  2024-04-27
  

Product Highlights:

The Nextera Rapid Capture Exome and Expanded Exome are all-in-one kits for library preparation and exome enrichment that allow researchers to identify coding variants up to 70% faster than other methods. This optimized exome delivers 45 Mb of expertly selected exonic content and requires as little as 4 Gb of sequencing.

Extend coverage to UTRs and miRNA with Expanded Exome

Nextera Rapid Capture Expanded Exome delivers 62 Mb of genomic content, including exons, untranslated regions (UTRs), and miRNA. This kit features a highly optimized probe set that delivers comprehensive coverage of exonic sequence.

Illumina provides example data sets to demonstrate the high uniformity and accuracy of the Nextera Rapid Capture Exome library prep kit. View the exome sequencing data.

Add on custom content to make Nextera Rapid Capture Exome even more powerful

Researchers can define custom content for this workflow using Nextera Rapid Capture Custom Enrichment. This custom assay allows researchers to rapidly interrogate those portions of the human genome most important to their specific research. Choose from a fully custom design or start from a defined content set, such as Nextera Rapid Capture Exome, and include areas of interest using add-on functionality. Learn More.

Find an up-to-date list of high-throughput automation vendors with robotic systems compatible with this library preparation kit

Specifications:

Assay Time5 hours total assay time
Hands-On Time4 hours
Input Quantity1 ug DNA (compatible with most large DNA genomes)
Mechanism of ActionMechanical fragmentation
MultiplexingUp to 96 dual-index combinations with HT (high-throughput) kit
Variant ClassSmall Insertions-Deletions (indels)
System CompatibilityHiSeq 2000,NextSeq 550,HiSeq 3000,NextSeq 500,HiSeq 2500,HiSeq 4000
Specialized Sample TypesLow Input
TechnologySequencing
Species CategoryHuman
Automation CapabilityLiquid Handling Robots
MethodExome Sequencing

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